--- title: "BD SWITZERLAND SARL Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search BD SWITZERLAND SARL recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/bd-switzerland-sarl/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # BD SWITZERLAND SARL recall records **12** reported ongoing 12 records in this archive. Latest source date Aug 19, 2026. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Aug 19, 2026 FDA device enforcement ### [BD Alaris Pump Infusion Sets 10561554\* 10885403232565 50885403232563 BD Alaris Pump Infusion Set, 15 Micron Filter, Back Check Valve, 3 SmartSite Y-sites 10015861A 1088540323262...](https://isitonrecall.com/recall/fda-device-z-3080-2026-bd-alaris-pump-infusion-sets-10561554-10885403232565-50885403232563-bd-alaris-pump-infusion-set-15-m/) Due to discrepancies in specific attributes in the performance data for infusion sets, which may lead to inappropriate pump performance. Class I Reported ongoing Distribution: U.S.: Nation-wide - AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MP, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, O... [Official source for BD Alaris Pump Infusion Sets 10561554\* 10885403232565 50885403232563 BD Alaris Pump Infusion Set,...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3080-2026%22) Jun 16, 2026 FDA device enforcement ### [60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code: 10885403236235 MaxPlus Ext Set w/Needleless and Y-Site REF MPX5305-C UDI-DI code: 10885403274619 9 IN Extension Set...](https://isitonrecall.com/recall/fda-device-z-2941-2026-60-in-non-dehp-minibore-extension-set-res-me2010-udi-di-code-10885403236235-maxplus-ext-set-w-needle/) Products may not have received adequate sterilization processing. Class II Reported ongoing Distribution: U.S.: AZ, CA, CO, FL, GA, IL, IN, KS, MD, MI, MN, MO, MS, NC, NV, NY, OH, OK, OR, PA, SD, TN, TX, UT, VA, WA O.U.S.: Canada [Official source for 60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code: 10885403236235 MaxPlus Ext Set w/Ne...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2941-2026%22) Jun 4, 2026 FDA device enforcement ### [MEDLINE 111 GRAVITY SET W/3 Needle Free Y-Sites REF DYNDTN0555 Catalog Number: SAM2461 UDI code: N/A Engineering Sample/Not for Human Use](https://isitonrecall.com/recall/fda-device-z-2654-2026-medline-111-gravity-set-w-3-needle-free-y-sites-ref-dyndtn0555-catalog-number-sam2461-udi-code-n-a-e/) Due to engineering sample labeled "Not for Human Use" being inadvertently shipped it the U.S. market. Class II Reported ongoing Distribution: U.S.: IL O.U.S: N/A [Official source for MEDLINE 111 GRAVITY SET W/3 Needle Free Y-Sites REF DYNDTN0555 Catalog Number: SAM2461 UDI code: ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2654-2026%22) May 21, 2026 FDA device enforcement ### [BD Connecta" BD Luer-Lok" 360 REF 394910 UDI-DI code: 00382903949106 BD Connecta" Stopcocks are used to administer fluids or medication through one or two different ports via an...](https://isitonrecall.com/recall/fda-device-z-2514-2026-bd-connecta-bd-luer-lok-360-ref-394910-udi-di-code-00382903949106-bd-connecta-stopcocks-are-used-to/) Due to stopcock issues when using the plastic luer-lok syringe, the connection at the Port C may over thread or continue to spin rather than tightening securely. This behavior has led some clinical users to perceive the connection as unstable. Class II Reported ongoing Distribution: U.S.: AK, AL, AR, AZ, CA, CO, DC, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, NE, NJ, NM, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WI, and WV. O.U.S.: Japan [Official source for BD Connecta" BD Luer-Lok" 360 REF 394910 UDI-DI code: 00382903949106 BD Connecta" Stopcocks are u...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2514-2026%22) Jun 16, 2025 FDA device enforcement ### [BD PhaSeal Injector Luer (N30C), REF: 515001 BD PhaSeal Injector Luer Lock (N35), REF: 515003 BD PhaSeal Injector Luer Lock (N35C), REF: 515004 BD PhaSeal Injector Lu63er Lock (...](https://isitonrecall.com/recall/fda-device-z-2453-2025-bd-phaseal-injector-luer-n30c-ref-515001-bd-phaseal-injector-luer-lock-n35-ref-515003-bd-phaseal-inj/) Closed system drug transfer devices were shipped to the U.S. market without a U.S. version of the instructions for use, which could be an issue if a healthcare professional is prompted to review it. Class II Reported ongoing Distribution: US Nationwide distribution including in the states of CA, WA, AL, OH, NC, GA, MA, IL, MO, AZ, PA, MS, MN, MI, TX, VA, IN, NV, CO, FL, WV, WI, NY, NJ, UT, MD, MT, NM, TN, HI, OK,... [Official source for BD PhaSeal Injector Luer (N30C), REF: 515001 BD PhaSeal Injector Luer Lock (N35), REF: 515003 BD ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2453-2025%22) May 12, 2025 FDA device enforcement ### [Alaris Pump Infusion Set: SmartSite Bag Access Non-Vented Bonded Texium With Priming Cap Back Check Valve 2 SmartSite Y-Sites, REF: 10013361T; SmartSite Bag Access Non-Vented Bo...](https://isitonrecall.com/recall/fda-device-z-1970-2025-alaris-pump-infusion-set-smartsite-bag-access-non-vented-bonded-texium-with-priming-cap-back-check-v/) Sterile, single use closed system drug transfer devices, standalone or on infusion sets or bonded syringes, may leak at the interface between the closed male luer component and the needle-free connector, which may cause procedure delay, treatment interrupti... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution including in the states of MA, CA, IL, AK, AL, MO, FL, VA, ME, NC, MD, IA, WI, AZ, CO, KY, IN, TX, AR, NJ, NY, MT, NE, TN, PA, GA, WA, KS,... [Official source for Alaris Pump Infusion Set: SmartSite Bag Access Non-Vented Bonded Texium With Priming Cap Back Che...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1970-2025%22) May 12, 2025 FDA device enforcement ### [BD Texium Needle-Free Syringe: 3 mL, REF: MY8003; 5 mL, REF: MY8005; 10 mL, REF: MY8010; 20 mL, REF: MY8020; 30 mL, REF: MY8030; 60 mL, REF: MY8060](https://isitonrecall.com/recall/fda-device-z-1971-2025-bd-texium-needle-free-syringe-3-ml-ref-my8003-5-ml-ref-my8005-10-ml-ref-my8010-20-ml-ref-my8020-30-m/) Sterile, single use closed system drug transfer devices, standalone or on infusion sets or bonded syringes, may leak at the interface between the closed male luer component and the needle-free connector, which may cause procedure delay, treatment interrupti... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution including in the states of MA, CA, IL, AK, AL, MO, FL, VA, ME, NC, MD, IA, WI, AZ, CO, KY, IN, TX, AR, NJ, NY, MT, NE, TN, PA, GA, WA, KS,... [Official source for BD Texium Needle-Free Syringe: 3 mL, REF: MY8003; 5 mL, REF: MY8005; 10 mL, REF: MY8010; 20 mL, R...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1971-2025%22) May 12, 2025 FDA device enforcement ### [BD Texium: 3 mL, REF: MY8003-0006; 5 mL, REF: MY8005-0006; 10 mL, REF: MY8010-0006; 20 mL, REF: MY8020-0006; 30 mL, REF: MY8030-0006; 60 mL, REF: MY8060-0006](https://isitonrecall.com/recall/fda-device-z-1972-2025-bd-texium-3-ml-ref-my8003-0006-5-ml-ref-my8005-0006-10-ml-ref-my8010-0006-20-ml-ref-my8020-0006-30-m/) Sterile, single use closed system drug transfer devices, standalone or on infusion sets or bonded syringes, may leak at the interface between the closed male luer component and the needle-free connector, which may cause procedure delay, treatment interrupti... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution including in the states of MA, CA, IL, AK, AL, MO, FL, VA, ME, NC, MD, IA, WI, AZ, CO, KY, IN, TX, AR, NJ, NY, MT, NE, TN, PA, GA, WA, KS,... [Official source for BD Texium: 3 mL, REF: MY8003-0006; 5 mL, REF: MY8005-0006; 10 mL, REF: MY8010-0006; 20 mL, REF: M...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1972-2025%22) May 12, 2025 FDA device enforcement ### [BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP, REF: 10012241-0500](https://isitonrecall.com/recall/fda-device-z-1973-2025-bd-texium-closed-male-luer-with-female-cap-ref-10012241-0500/) Sterile, single use closed system drug transfer devices, standalone or on infusion sets or bonded syringes, may leak at the interface between the closed male luer component and the needle-free connector, which may cause procedure delay, treatment interrupti... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution including in the states of MA, CA, IL, AK, AL, MO, FL, VA, ME, NC, MD, IA, WI, AZ, CO, KY, IN, TX, AR, NJ, NY, MT, NE, TN, PA, GA, WA, KS,... [Official source for BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP, REF: 10012241-0500](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1973-2025%22) May 12, 2025 FDA device enforcement ### [BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP, REF: 10012241; BD TEXIUM (China), REF: 10012241 CHINA](https://isitonrecall.com/recall/fda-device-z-1974-2025-bd-texium-closed-male-luer-with-female-cap-ref-10012241-bd-texium-china-ref-10012241-china/) Sterile, single use closed system drug transfer devices, standalone or on infusion sets or bonded syringes, may leak at the interface between the closed male luer component and the needle-free connector, which may cause procedure delay, treatment interrupti... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution including in the states of MA, CA, IL, AK, AL, MO, FL, VA, ME, NC, MD, IA, WI, AZ, CO, KY, IN, TX, AR, NJ, NY, MT, NE, TN, PA, GA, WA, KS,... [Official source for BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP, REF: 10012241; BD TEXIUM (China), REF: 10012241 CHINA](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1974-2025%22) Feb 20, 2025 FDA device enforcement ### [BD Connecta BD Luer-Lok 360, REF 394910 UDI-DI code: 00382903949106 Connecta¿ Plus 1 and Connecta¿ Plus 3 2-way and 3-way Stopcocks are control valves for use in IV. therapy and...](https://isitonrecall.com/recall/fda-device-z-1509-2025-bd-connecta-bd-luer-lok-360-ref-394910-udi-di-code-00382903949106-connecta-plus-1-and-connecta-plus/) Due to specific lots of luer-lok devices were shipped to the U.S. market with an Outside US Instruction for Use (IFU) Class II Reported ongoing Distribution: U.S.: AK, AL, AR, AZ, CA, CO, FL, GA, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, NE, NJ, NM, NV, OH, OK, OR, PA, SC, TN. TX, UT, VA, WA, WV O.U.S.: N/A [Official source for BD Connecta BD Luer-Lok 360, REF 394910 UDI-DI code: 00382903949106 Connecta¿ Plus 1 and Connecta...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1509-2025%22) Apr 18, 2024 FDA device enforcement ### [Alaris Pump Infusion Set Low Sorbing Tubing (PE Lined) Back Check Valve 2 SmartSite Y Sites REF 10013072 Tubing set used for delivery of fluids, medication, blood and blood prod...](https://isitonrecall.com/recall/fda-device-z-1944-2024-alaris-pump-infusion-set-low-sorbing-tubing-pe-lined-back-check-valve-2-smartsite-y-sites-ref-100130/) Due to infusion set tubing drip chamber becoming detached from the tubing potentially causing delays in treatment, or unintentionally exposing users to harsh infusates. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of AR, CA, CO, IL, KS, MA, ME, NJ, NY, PA, SD, WA and WI. The country of Canada. [Official source for Alaris Pump Infusion Set Low Sorbing Tubing (PE Lined) Back Check Valve 2 SmartSite Y Sites REF 1...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1944-2024%22) ## Reasons in these listed records - Due to discrepancies in specific attributes in the performance data for infusion sets, which may lead to inappropriate pump performance. - Products may not have received adequate sterilization processing. - Due to engineering sample labeled "Not for Human Use" being inadvertently shipped it the U.S. market. - Due to stopcock issues when using the plastic luer-lok syringe, the connection at the Port C may over thread or continue to spin rather than tightening securely. This behavior has led some clinical users to perceive the connection as unstable. These examples come from this result page and are not a ranking of every recall reason. ## Checking BD SWITZERLAND SARL ### Is there a recall on bd switzerland sarl right now? This archive contains 12 records, including 12 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search BD SWITZERLAND SARL](https://isitonrecall.com/check/?q=BD%20SWITZERLAND%20SARL) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)